meddevicedb.com FDA Device Reference

TELEMETRY SYSTEM

K823906 Class II Traditional
Decision Date
1983-03-09
Sponsor / Applicant
Transkinetic Systems, Inc.

Technical Specification

510(k) Submission ID K823906
Product Code DRG
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.2910
Decision Date 1983-03-09
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

TELEMETRY SYSTEM received FDA 510(k) clearance under submission number K823906, sponsored by Transkinetic Systems, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 1983-03-09.

Classification & Regulation

This clearance is catalogued under FDA product code DRG and 21 CFR 870.2910, within the Cardiovascular review panel as a Class II device.